-
1
-
-
0000572881
-
A study of 1-aryl cyclohexylamine for anesthesia
-
Greifenstein, F. E., Yoshitake, J., DeVault, M., and Gajewski, J. E. (1958) A study of 1-aryl cyclohexylamine for anesthesia. Anesth. Analg. 37, 283-294.
-
(1958)
Anesth. Analg
, vol.37
, pp. 283-294
-
-
Greifenstein, F.E.1
Yoshitake, J.2
DeVault, M.3
Gajewski, J.E.4
-
2
-
-
0017184603
-
Psychiatric sequelae of phencyclidine abuse
-
Fauman, B., Aldinger, G., Fauman, M., and Rosen, P. (1976) Psychiatric sequelae of phencyclidine abuse. Clin. Toxicol. 9, 529-538.
-
(1976)
Clin. Toxicol
, vol.9
, pp. 529-538
-
-
Fauman, B.1
Aldinger, G.2
Fauman, M.3
Rosen, P.4
-
3
-
-
0019476199
-
Metabolic disposition and irreversible binding of phencyclidine in rats
-
Law, F. C. P. (1981) Metabolic disposition and irreversible binding of phencyclidine in rats. Toxicol. Appl. Pharmacol. 57, 263-272.
-
(1981)
Toxicol. Appl. Pharmacol
, vol.57
, pp. 263-272
-
-
Law, F.C.P.1
-
4
-
-
0020322386
-
Metabolic formation of iminium species: Metabolism of phencyclidine
-
Ward, D., Kalir, A., Trevor, A., Adams, J., and Baillie, T., Jr. (1982) Metabolic formation of iminium species: Metabolism of phencyclidine. J. Med. Chem. 25, 491-492.
-
(1982)
J. Med. Chem
, vol.25
, pp. 491-492
-
-
Ward, D.1
Kalir, A.2
Trevor, A.3
Adams, J.4
Baillie Jr., T.5
-
5
-
-
0020378847
-
Metabolism of phencyclidine: The role of iminium ion formation in covalent binding to rabbit microsomal protein
-
Ward, D. P., Trevor, A. J., Kalir, A., Adams, J. D., and Baillie, T. A., Jr. (1982) Metabolism of phencyclidine: The role of iminium ion formation in covalent binding to rabbit microsomal protein. Drug Metab. Dispos. 10, 690-695.
-
(1982)
Drug Metab. Dispos
, vol.10
, pp. 690-695
-
-
Ward, D.P.1
Trevor, A.J.2
Kalir, A.3
Adams, J.D.4
Baillie Jr., T.A.5
-
6
-
-
0021734894
-
Metabolism-dependent inactivation of liver microsomal enzymes by phencyclidine
-
Hoag, M. K. P., Trevor, A. J., Asscher, Y., and Weissman, J., Jr. (1984) Metabolism-dependent inactivation of liver microsomal enzymes by phencyclidine. Drug Metab. Dispos. 12, 371-375.
-
(1984)
Drug Metab. Dispos
, vol.12
, pp. 371-375
-
-
Hoag, M.K.P.1
Trevor, A.J.2
Asscher, Y.3
Weissman Jr., J.4
-
7
-
-
0023201596
-
Phencyclidine iminium ion: NADPH-dependent metabolism, covalent binding to macromolecules, and inactivation of cytochrome(s) P-450
-
Hoag, M. K. P., Trevor, A. J., and Kalir, A., Jr. (1987) Phencyclidine iminium ion: NADPH-dependent metabolism, covalent binding to macromolecules, and inactivation of cytochrome(s) P-450. Drug Metab. Dispos. 15, 485-490.
-
(1987)
Drug Metab. Dispos
, vol.15
, pp. 485-490
-
-
Hoag, M.K.P.1
Trevor, A.J.2
Kalir Jr., A.3
-
8
-
-
0024545859
-
Selective mechanism-based inactivation of the major phenobarbital-inducible P-450 cytochrome from rabbit liver by phencyclidine and its oxidation product, the iminium compound
-
Osawa, Y., and Coon, M. J. (1989) Selective mechanism-based inactivation of the major phenobarbital-inducible P-450 cytochrome from rabbit liver by phencyclidine and its oxidation product, the iminium compound. Drug Metab. Dispos. 17, 7-13.
-
(1989)
Drug Metab. Dispos
, vol.17
, pp. 7-13
-
-
Osawa, Y.1
Coon, M.J.2
-
9
-
-
0029165394
-
Mechanism-based inactivation of rat liver cytochrome P4502B1 by phencyclidine and its oxidative product, the iminium ion
-
Crowley, J. R., and Hollenberg, P. F. (1995) Mechanism-based inactivation of rat liver cytochrome P4502B1 by phencyclidine and its oxidative product, the iminium ion. Drug Metab. Dispos. 23, 786-793.
-
(1995)
Drug Metab. Dispos
, vol.23
, pp. 786-793
-
-
Crowley, J.R.1
Hollenberg, P.F.2
-
10
-
-
0031026767
-
Metabolic activation of cytochrome P4502B1 by phencyclidine: Immunochemical and radiochemical analyses of the protective effects of glutathione
-
Sharma, U., Roberts, E. S., Kent, U. M., Owens, S. M., and Hollenberg, P. F. (1997) Metabolic activation of cytochrome P4502B1 by phencyclidine: Immunochemical and radiochemical analyses of the protective effects of glutathione. Drug Metab. Dispos. 25, 243-250.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 243-250
-
-
Sharma, U.1
Roberts, E.S.2
Kent, U.M.3
Owens, S.M.4
Hollenberg, P.F.5
-
11
-
-
0037671381
-
The mechanism-based inactivation of human cytochrome P450 2B6 by phencyclidine
-
Jushchyshyn, M. I., Kent, U. M., and Hollenberg, P. F. (2003) The mechanism-based inactivation of human cytochrome P450 2B6 by phencyclidine. Drug Metab. Dispos. 31, 46-52.
-
(2003)
Drug Metab. Dispos
, vol.31
, pp. 46-52
-
-
Jushchyshyn, M.I.1
Kent, U.M.2
Hollenberg, P.F.3
-
12
-
-
33344475261
-
Selective pathways for the metabolism of phencyclidine by cytochrome P450 2B enzymes: Identification of electrophilic metabolites, glutathione, and N-acetyl cysteine adducts
-
Shebley, M., Jushchyshyn, M. I., and Hollenberg, P. F. (2006) Selective pathways for the metabolism of phencyclidine by cytochrome P450 2B enzymes: Identification of electrophilic metabolites, glutathione, and N-acetyl cysteine adducts. Drug Metab. Dispos. 34, 375-383.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 375-383
-
-
Shebley, M.1
Jushchyshyn, M.I.2
Hollenberg, P.F.3
-
13
-
-
33747824131
-
Mechanism of inactivation of human cytochrome P450 2B6 by phencyclidine
-
Jushchyshyn, M. I., Wahlstrom, J. L., Hollenberg, P. F., and Wienkers, L. C. (2006) Mechanism of inactivation of human cytochrome P450 2B6 by phencyclidine. Drug Metab. Dispos. 34, 1523-1529.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 1523-1529
-
-
Jushchyshyn, M.I.1
Wahlstrom, J.L.2
Hollenberg, P.F.3
Wienkers, L.C.4
-
14
-
-
84910569482
-
Reactive metabolites of phencyclidine and covalent binding to microsomal proteins
-
Kamenca, J. M, Domino, E. F, and Geneste, P, Eds, pp, NPP Books, Ann Arbor, MI
-
Kalir, A., Trevor, A. J., Ward, D. P., Adams, J. D., Baillie, T. A., and Castagnoli, N., Jr. (1983) Reactive metabolites of phencyclidine and covalent binding to microsomal proteins. In Phencyclidine and Related Arylcyclohexylamines: Present and Future Applications (Kamenca, J. M., Domino, E. F., and Geneste, P., Eds.) pp 267-278, NPP Books, Ann Arbor, MI.
-
(1983)
Phencyclidine and Related Arylcyclohexylamines: Present and Future Applications
, pp. 267-278
-
-
Kalir, A.1
Trevor, A.J.2
Ward, D.P.3
Adams, J.D.4
Baillie, T.A.5
Castagnoli Jr., N.6
-
15
-
-
0019968939
-
Chemical synthesis and molecular pharmacology of hydroxylated 1-(1-phenylcyclohexyl)piperidine derivatives
-
Kamenka, J. M., Chiche, B., Goudal, R., Geneste, P., Vignon, J., Vincent, J. P., and Lazdunski, M. (1982) Chemical synthesis and molecular pharmacology of hydroxylated 1-(1-phenylcyclohexyl)piperidine derivatives. J. Med. Chem. 25, 431-435.
-
(1982)
J. Med. Chem
, vol.25
, pp. 431-435
-
-
Kamenka, J.M.1
Chiche, B.2
Goudal, R.3
Geneste, P.4
Vignon, J.5
Vincent, J.P.6
Lazdunski, M.7
-
16
-
-
35848950733
-
Preparation of cyclohexenylphenols
-
Jpn. Kokai Tokkyo Koho JP 2002212123
-
Hiramine, T., Ono, H., Isoda, Y., Yao, K., and Kojima, H. (2002) Preparation of cyclohexenylphenols. Jpn. Kokai Tokkyo Koho JP 2002212123.
-
(2002)
-
-
Hiramine, T.1
Ono, H.2
Isoda, Y.3
Yao, K.4
Kojima, H.5
-
17
-
-
0020684703
-
Quantitation of phencyclidine in serum by enzyme immunoassay: Results in 405 patients
-
Walberg, C. B., McCarron, M. M., and Schulze, B. W. (1983) Quantitation of phencyclidine in serum by enzyme immunoassay: results in 405 patients. J. Anal. Toxicol. 7, 106-110.
-
(1983)
J. Anal. Toxicol
, vol.7
, pp. 106-110
-
-
Walberg, C.B.1
McCarron, M.M.2
Schulze, B.W.3
-
18
-
-
0036179579
-
(+)-N-3-Benzyl-nirvanol and (-)-N-3-benzyl- phenobarbital: New potent and selective in vitro inhibitors of CYP2C19
-
Suzuki, H., Kneller, M. B., Haining, R. L., Trager, W. F., and Rettie, A. E. (2002) (+)-N-3-Benzyl-nirvanol and (-)-N-3-benzyl- phenobarbital: new potent and selective in vitro inhibitors of CYP2C19. Drug Metab. Dispos. 30, 235-239.
-
(2002)
Drug Metab. Dispos
, vol.30
, pp. 235-239
-
-
Suzuki, H.1
Kneller, M.B.2
Haining, R.L.3
Trager, W.F.4
Rettie, A.E.5
-
19
-
-
0037369493
-
Verification of the selectivity of (+)-N-3-benzylnirvanol as a CYP2C19 inhibitor
-
Walsky, R. L., and Obach, R. S. (2003) Verification of the selectivity of (+)-N-3-benzylnirvanol as a CYP2C19 inhibitor. Drug Metab. Dispos. 31, 343.
-
(2003)
Drug Metab. Dispos
, vol.31
, pp. 343
-
-
Walsky, R.L.1
Obach, R.S.2
-
20
-
-
0023888337
-
Metabolism studies on phencyclidine: Characterization of a phencyclidine iminium ion metabolite
-
Hoag, M. L. P., Schmidt-Peetz, M., Lampen, P., Trevor, A. J., and Castagnoli, N., Jr. (1988) Metabolism studies on phencyclidine: characterization of a phencyclidine iminium ion metabolite. Chem. Res. Toxicol. 1, 128-131.
-
(1988)
Chem. Res. Toxicol
, vol.1
, pp. 128-131
-
-
Hoag, M.L.P.1
Schmidt-Peetz, M.2
Lampen, P.3
Trevor, A.J.4
Castagnoli Jr., N.5
-
21
-
-
0023874837
-
Hydroxy metabolites of phencyclidine: Identification and quantitation of two novel metabolites
-
Gole, D. J., Pirat, J.-L., Kamenka, J.-M., and Domino, E. F. (1988) Hydroxy metabolites of phencyclidine: Identification and quantitation of two novel metabolites. Drug Metab. Dispos. 16, 386-391.
-
(1988)
Drug Metab. Dispos
, vol.16
, pp. 386-391
-
-
Gole, D.J.1
Pirat, J.-L.2
Kamenka, J.-M.3
Domino, E.F.4
-
22
-
-
0022392310
-
Biotransformation of phencyclidine
-
Holsztynska, E. J., and Domino, E. F. (1986) Biotransformation of phencyclidine. Drug Metab. Rev. 16, 285-320.
-
(1986)
Drug Metab. Rev
, vol.16
, pp. 285-320
-
-
Holsztynska, E.J.1
Domino, E.F.2
-
23
-
-
0030984837
-
Metabolism of phencyclidine by human liver microsomes
-
Laurenzana, E. M., and Owens, S. M. (1997) Metabolism of phencyclidine by human liver microsomes. Drug Metab. Dispos. 25, 557-563.
-
(1997)
Drug Metab. Dispos
, vol.25
, pp. 557-563
-
-
Laurenzana, E.M.1
Owens, S.M.2
-
24
-
-
0017088005
-
Metabolites of phencyclidine
-
Wong, L. K., and Biemann, K. (1976) Metabolites of phencyclidine. Clin. Toxicol. 9, 583-591.
-
(1976)
Clin. Toxicol
, vol.9
, pp. 583-591
-
-
Wong, L.K.1
Biemann, K.2
-
26
-
-
0023201330
-
A phenolic metabolite of phencyclidine. The formation of a pharmacologically active metabolite by rat liver microsomes
-
Ohta, S., Masumoto, H., Takeuchi, K., and Hirobe, M. (1987) A phenolic metabolite of phencyclidine. The formation of a pharmacologically active metabolite by rat liver microsomes. Drug Metab. Dispos. 15, 583-584.
-
(1987)
Drug Metab. Dispos
, vol.15
, pp. 583-584
-
-
Ohta, S.1
Masumoto, H.2
Takeuchi, K.3
Hirobe, M.4
-
27
-
-
0020418757
-
In vitro metabolism of 1-phenyl-1-cyclohexene, a pyrolysis product of phencyclidine
-
Martin, B. R., Bailey, B. B., Awaya, H., May, E. L., and Narasimhachari, N. (1982) In vitro metabolism of 1-phenyl-1-cyclohexene, a pyrolysis product of phencyclidine. Drug Metab. Dispos. 10, 685-689.
-
(1982)
Drug Metab. Dispos
, vol.10
, pp. 685-689
-
-
Martin, B.R.1
Bailey, B.B.2
Awaya, H.3
May, E.L.4
Narasimhachari, N.5
-
28
-
-
0028930981
-
o-Methoxy-4-alkylphenols that form quinone methides of intermediate reactivity are the most toxic in rat liver slices
-
Thompson, D. C., Perera, K., Krol, E. S., and Bolton, J. L. (1995) o-Methoxy-4-alkylphenols that form quinone methides of intermediate reactivity are the most toxic in rat liver slices. Chem. Res. Toxicol. 8, 323-327.
-
(1995)
Chem. Res. Toxicol
, vol.8
, pp. 323-327
-
-
Thompson, D.C.1
Perera, K.2
Krol, E.S.3
Bolton, J.L.4
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